Page last updated: 2024-12-07

perseitol

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth

Description

perseitol: RN given refers to (D-glycero-D-galacto)-isomer [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

perseitol : A heptitol that is heptane-1,2,3,4,5,6,7-heptol that has R-configuration at positions 2, 3, 4 and 5, and S-configuration at position 6. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID441436
CHEBI ID8029
SCHEMBL ID532907
SCHEMBL ID4245457
MeSH IDM0085239

Synonyms (22)

Synonym
perseitol
C08255
527-06-0
(2s,3r,5r,6r)-heptane-1,2,3,4,5,6,7-heptol
unii-565po82at6
nsc 1976
einecs 208-406-1
565po82at6 ,
l-glycero-d-manno-heptitol
CHEBI:8029
(2r,3r,4r,5r,6s)-heptane-1,2,3,4,5,6,7-heptol
perseit
CCG-214144
SCHEMBL532907
SCHEMBL4245457
W-202992
(2r,3r,5r,6s)-heptane-1,2,3,4,5,6,7-heptol
Q27089371
Q11815734
perseitol from avocardo
BS-28631
AKOS040759766

Research Excerpts

Bioavailability

ExcerptReferenceRelevance
" Bioavailability was calculated as F=AUC by gavage/AUC by injection, where AUC is the area under the curve of plasma probe concentration vs."( Intestinal passive absorption of water-soluble compounds by sparrows: effect of molecular size and luminal nutrients.
Caviedes-Vidal, E; Chediack, JG; Fasulo, V; Karasov, WH; Yamin, LJ, 2003
)
0.32
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (1)

Assay IDTitleYearJournalArticle
AID1159550Human Phosphogluconate dehydrogenase (6PGD) Inhibitor Screening2015Nature cell biology, Nov, Volume: 17, Issue:11
6-Phosphogluconate dehydrogenase links oxidative PPP, lipogenesis and tumour growth by inhibiting LKB1-AMPK signalling.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (13)

TimeframeStudies, This Drug (%)All Drugs %
pre-19903 (23.08)18.7374
1990's3 (23.08)18.2507
2000's4 (30.77)29.6817
2010's3 (23.08)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (7.14%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other13 (92.86%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]